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用甲氧明和去氧肾上腺素刺激α1-肾上腺素能受体对家兔窦房结自律性细胞的影响。

Effect of alpha 1-adrenoceptor stimulation with methoxamine and phenylephrine on spontaneously beating rabbit sino-atrial node cells.

作者信息

Satoh H, Hashimoto K

机构信息

Department of Pharmacology, Yamanashi Medical College, Japan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1988 Apr;337(4):415-22. doi: 10.1007/BF00169533.

Abstract

Effects of methoxamine and phenylephrine on the action potential and the membrane currents in spontaneously beating rabbit sino-atrial node cells were examined by means of a two-microelectrode voltage-clamp technique. Both methoxamine and phenylephrine (10(-4) mol/l) prolonged the cycle length (CL) and the action potential duration (APD), significantly. At concentrations higher than 3 x 10(-4) mol/l, phenylephrine increased the maximum rate of rise of action potential (Vmax) but methoxamine reduced it. Both agents depolarized the maximum diastolic potential (MDP). These changes in the action potential parameters occurred in a concentration-dependent manner. In the presence of phentolamine (10(-5) mol/l), methoxamine (3 x 10(-4) mol/l) did not modify the action potential parameters. Also, phenylephrine did not affect them during exposure to phentolamine (10(-5) mol/l) and pindolol (10(-7) mol/l). In voltage-clamp experiments, at 10(-3) mol/l both methoxamine and phenylephrine slightly increased the slow inward current (Isi), but decreased the time-dependent outward current (Ik). The steady-state activation variable of Ik (p infinity) was unaffected by these agents. The hyperpolarization-activated current (Ih) was suppressed in the presence of methoxamine, but enhanced in the presence of phenylephrine. An additional application of pindolol (10(-7) mol/l) during exposure to phenylephrine (10(-3) mol/l) depressed the action potential amplitude (APA) and Vmax, and prolonged CL slightly. Under the same condition, all the membrane currents (Isi, Ik and Ih) were decreased. In addition, the time courses of decay for Isi were not modified in the absence and the presence of phenylephrine (10(-3) mol/l) and phenylephrine plus pindolol (10(-7) mol/l).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用双微电极电压钳技术,研究了甲氧明和去氧肾上腺素对家兔窦房结自律细胞动作电位及膜电流的影响。甲氧明和去氧肾上腺素(10⁻⁴mol/L)均能显著延长心动周期长度(CL)和动作电位时程(APD)。当浓度高于3×10⁻⁴mol/L时,去氧肾上腺素可增加动作电位最大上升速率(Vmax),而甲氧明则使其降低。两种药物均可使最大舒张电位(MDP)去极化。动作电位参数的这些变化呈浓度依赖性。在酚妥拉明(10⁻⁵mol/L)存在的情况下,甲氧明(3×10⁻⁴mol/L)不改变动作电位参数。同样,在酚妥拉明(10⁻⁵mol/L)和吲哚洛尔(10⁻⁷mol/L)作用期间,去氧肾上腺素对其也无影响。在电压钳实验中,10⁻³mol/L的甲氧明和去氧肾上腺素均可轻微增加慢内向电流(Isi),但减少时间依赖性外向电流(Ik)。Ik的稳态激活变量(p∞)不受这些药物影响。甲氧明存在时超极化激活电流(Ih)受到抑制,而去氧肾上腺素存在时则增强。在去氧肾上腺素(10⁻³mol/L)作用期间额外应用吲哚洛尔(10⁻⁷mol/L)可降低动作电位幅度(APA)和Vmax,并轻微延长CL。在相同条件下,所有膜电流(Isi、Ik和Ih)均降低。此外,在有无去氧肾上腺素(10⁻³mol/L)以及去氧肾上腺素加吲哚洛尔(10⁻⁷mol/L)的情况下,Isi的衰减时间进程未发生改变。(摘要截短于250字)

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